Hypothesis
Neurocardiogenic syncope: a model for SIDS
a Department
of Paediatrics, Rotunda Hospital and The Children's Hospital, Temple
Street, Dublin l, Republic of Ireland, b Department of Paediatrics, Castlebar General
Hospital, Castlebar, Co Mayo, Republic of Ireland
Correspondence to: Professor Matthews.
Accepted 31 December 1997
A 51/2 month old male infant who had suffered three
acute life threatening episodes was admitted for overnight sleep
studies but was found dead after their completion while still in
hospital. A necropsy classified the cause of death as sudden infant
death syndrome (SIDS). The sleep studies had shown no periods of apnoea (> 20 seconds) or bradycardia (< 90 beats/min), and a rapid
response to nasal occlusion (5 seconds). However, autonomic function
during sleep was poor, with reduced heart rate variability (6 beats/min v control 24 beats/min, SD 6.2) and postural hypotension
(a 12-14% fall in resting systolic blood pressure) associated with a
fall in heart rate when tilted to a vertical position. Postural
hypotension with bradycardia occurs in adults with unexplained syncopal
episodes and is called a neurocardiac reflex. It involves poor
vasomotor tone with peripheral pooling of blood, a consequent reduction in central venous return and cardiac distension, and in some
individuals a neurally mediated bradycardia, as seen in this infant,
rather than the expected tachycardia. A progressive bradycardia is the predominant mechanism of death seen in SIDS infants dying on
cardiorespiratory monitors at home. This case suggests that a
neurocardiac reflex occurs in infants, may have been involved in this
infant's death, and deserves further study in the context of SIDS.
© 1998 by Archives of Disease in Childhood
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